Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Triamcinolone acetonide
Drug ID BADD_D02272
Description Triamcinolone is a corticosteroid used to treat various inflammatory conditions in the body from allergic rhinitis to acute exacerbations of multiple sclerosis.[L8255] Triamcinolone can be used as a one time adjunct treatment of osteoarthritic knee pain,[L8264] or first line as a topical treatment of corticosteroid responsive dermatoses.[L8249] Triamcinolone is more commonly seen in the forms triamcinolone hexacetonide, triamcinolone acetonide, and triamcinolone diacetate.[L8246,L8249,L8252,L8255,L8258,L8261,L8264] Triamcinolone was granted FDA approval on 3 December 1957.[L8243] In October 2021, a suspension of triamcinolone acetonide was approved for suprachoroidal injection - the first suprachoroidal injection to receive FDA approval[L38973] - for the treatment of patients with macular edema associated with uveitis.[L38963]
Indications and Usage Triamcinolone hexacetonide injections are indicated for intralesional administration in alopecia areata, discoid lupus erythematosus, keloids, and necrobiosis lipoidica diabeticorum.[L8246] This formulation can also be used for localized hypertrophic infiltrated inflammatory lesions of granuloma annulare, lichen planus, lichen simplex chronicus, and psoriatic plaques.[L8246] Triamcinolone acetonide spray and cream are indicated for the treatment of inflammatory and pruritic manifestations of corticosteroid responsive dermatoses.[L8249,L8258] A triamcinolone acetonide 10mg/mL or 40mg/mL injection is indicated intra-articularly for acute gouty arthritis, acute and subacute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis, and synovitis of osteoarthritis.[L8252,L8255] The same 10mg/mL injection is indicated by the intralesional route for the treatment of alopecia areata, discoid lupus erythematosus, keloids, necrobiosis lipoidica diabeticorum, and tumors of an aponeurosis or tendon.[L8252] This formulation can also be used for localized hypertrophic infiltrated inflammatory lesions of granuloma annulare, lichen planus, lichen simplex chronicus, and psoriatic plaques.[L8252] The 40mg/mL injection is indicated intramuscularly for controlling severe allergic conditions such as asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity, perennial or seasonal allergic rhinitis, serum sickness, and transfusion reactions; treatment of bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, Stevens-Johnson syndrome, congenital adrenal hyperplasia, hypercalcemia in cancer, nonsuppurative thyroiditis, autoimmune hemolytic anemia, Diamond-Blackfan anemia, pure red cell aplasia, secondary thrombocytopenia, trichinosis, tuberculous meningitis, acute exacerbations of multiple sclerosis or cerebral edema, sympathetic ophthalmia, temporal arteritis, uveitis, ocular inflammation, berylliosis, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis, dermatomyositis, polymyositis, and systemic lupus erythematosus; adjunct treatment of adrenocortical insufficiency, regional enteritis, ulcerative colitis, fulminating or disseminated pulmonary tuberculosis, acute gouty arthritis, acute rheumatic carditis, ankylosing spondylitis, psoriatic arthritis, rheumatoid arthritis; palliative management of leukemia and lymphoma; induction of diuresis or remission of proteinuria in idiopathic nephrotic syndrome or lupus erythematosus.[L8255] A triamcinolone intravitreal injection is indicated for the treatment of sympathetic ophthalmia, temporal arteritis, uveitis, and ocular inflammatory conditions.[L8261] The intravitreal injection is also used for visualization during vitrectomy.[L8261] An extended release suspension is indicated intra-articularly for management of pain in osteoarthritis of the knee.[L8264] A triamcinolone acetonide suspension for injection into the suprachoroidal space is indicated for the treatment of macular edema associated with uveitis.[L38963]
Marketing Status approved; vet_approved
ATC Code D07AB09; D07XB02; C05AA12; S01BA05; R03BA06; R01AD11; A01AC01; H02AB08
DrugBank ID DB00620
KEGG ID D00983
MeSH ID D014222
PubChem ID 6436
TTD Drug ID Not Available
NDC Product Code 76420-085; 76420-222; 81298-5781; 46439-8703; 41167-5800; 41250-443; 0168-0006; 50090-3802; 51672-1335; 0316-0165; 61919-619; 63629-8782; 63629-8785; 64380-800; 67457-621; 68071-2743; 70518-2403; 70518-3373; 71205-009; 71205-033; 0713-0226; 0713-0229; 0713-0655; 0003-0293; 76003-1145; 82298-123; 16714-987; 36800-621; 45865-898; 50090-2244; 51672-1282; 53002-9770; 63629-8783; 68071-1872; 68788-7501; 68788-8350; 70121-1653; 70121-1654; 70752-140; 71205-108; 71205-627; 72162-1832; 81298-5783; 0003-0494; 49452-7900; 51552-0033; 16714-150; 33342-333; 41163-443; 0168-0002; 44118-711; 45802-045; 50090-0293; 50090-0295; 50090-2106; 55150-384; 0316-0175; 61919-650; 63187-661; 63629-2406; 63629-8780; 63629-8784; 67877-251; 68071-2339; 68071-2736; 70121-1049; 70121-1168; 70518-2285; 55150-385; 55910-280; 59088-730; 62011-0320; 0363-0811; 63187-025; 63187-214; 63629-2407; 63629-9573; 67877-318; 68788-7797; 70121-1651; 70518-2393; 70529-048; 0703-0245; 80425-0262; 12516-1508; 12516-1509; 57582-018; 65089-0008; 71161-135; 16714-267; 30142-443; 0113-0443; 40032-097; 0168-0004; 45802-055; 50090-1444; 52817-811; 53002-9333; 63187-870; 64380-901; 64980-320; 68071-1623; 68788-7048; 71205-451; 71565-040; 72189-039; 72189-277; 0703-0243; 0713-0228; 76420-203; 51927-0306; 10631-093; 21130-443; 33342-329; 33342-332; 35573-404; 45802-063; 45802-064; 50090-6533; 63629-8708; 64380-870; 67457-622; 67457-623; 68071-2294; 68788-8386; 70121-1657; 70752-130; 46439-8730; 62991-1156; 16714-985; 24470-922; 33342-331; 45802-817; 49035-443; 50090-0362; 50090-5980; 51672-1267; 0316-0170; 61919-594; 63629-9574; 64380-802; 67877-317; 68462-131; 68788-8356; 68788-8457; 70752-129; 0713-0676; 12516-1510; 67438-045; 24208-040; 42571-385; 0168-0003; 45802-049; 45802-065; 50090-0163; 50090-0256; 51672-1284; 53002-9120; 63187-053; 68462-797; 70000-0204; 70121-1655; 70518-3689; 70677-1023; 71205-038; 46439-8742; 49076-6701; 52128-173; 52945-068; 73301-011; 76420-162; 11673-717; 16714-140; 16714-268; 16714-986; 30142-813; 0168-0005; 45802-054; 51862-290; 53002-9334; 59088-733; 59779-746; 63187-495; 63629-8778; 63629-8781; 63981-443; 64380-801; 64980-429; 68788-7814; 70121-1169; 70518-2938; 71205-124; 72288-443; 0703-0241; 0713-0225; 74157-901; 76420-220; 0003-0315; 81298-5785; 22552-0032; 60722-3012; 16714-130; 33342-327; 46122-385; 50090-2658; 50090-6547; 53002-0151; 63629-8456; 63629-8707; 63629-8779; 63629-8841; 64380-871; 68462-798; 68788-7506; 70121-1652; 70518-1094; 71428-010; 0065-0543; 38779-0011; 51927-0134; 63275-9943; 33342-328; 37808-443; 45802-109; 46287-010; 49999-150; 50090-6211; 53002-9331
UNII F446C597KA
Synonyms Triamcinolone Acetonide | Acetonide, Triamcinolone | Cinonide | Tricort-40 | Tricort 40 | Tricort40 | Kenalog | Kenalog 40 | Azmacort | Kenacort A
Chemical Information
Molecular Formula C24H31FO6
CAS Registry Number 76-25-5
SMILES CC1(OC2CC3C4CCC5=CC(=O)C=CC5(C4(C(CC3(C2(O1)C(=O)CO)C)O)F)C)C
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Hypereosinophilic syndrome01.02.04.0050.000041%Not Available
Localised oedema14.05.06.009; 08.01.07.011; 02.05.04.0060.000087%
Oesophagitis ulcerative07.04.05.003--Not Available
Lipodystrophy acquired23.07.01.003; 14.08.04.0080.000087%Not Available
Pneumomediastinum22.09.03.0040.000027%Not Available
Lupus-like syndrome10.04.03.003; 23.03.02.004; 15.06.02.004--Not Available
Contusion24.07.06.001; 23.03.11.002; 12.01.06.001; 15.03.05.007--
Foreign body sensation in eyes06.01.01.006--Not Available
Rhinalgia22.12.03.0200.000093%Not Available
Injection site discolouration23.03.03.046; 12.07.03.038; 08.02.03.0380.000598%Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.015--Not Available
Anterior chamber flare06.04.10.003--Not Available
Eye pruritus06.04.05.006--Not Available
Ocular discomfort06.08.03.0080.000060%Not Available
Respiratory tract congestion22.02.07.003--Not Available
Nasal discomfort22.12.03.012--Not Available
Detachment of retinal pigment epithelium06.09.03.0110.000027%Not Available
Nerve injury17.02.10.007; 12.01.12.002--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Application site swelling12.07.01.027; 08.02.01.0270.000139%Not Available
Injection site swelling12.07.03.018; 08.02.03.0170.000074%Not Available
Type IV hypersensitivity reaction10.01.03.0220.000027%Not Available
Vascular occlusion24.04.02.0150.000041%Not Available
Growth retardation15.03.05.016; 14.03.02.031; 05.03.02.007--
Anterior chamber cell06.04.10.0010.000055%Not Available
Affect lability19.04.01.001--Not Available
Corneal thinning06.06.03.0090.000027%Not Available
Anterior chamber inflammation06.04.10.0020.000027%Not Available
Skin burning sensation17.02.06.009; 23.03.03.0210.000093%Not Available
Injection site calcification12.07.03.043; 08.02.03.0430.000068%Not Available
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